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bummblle bummblle
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6 years ago
In familial hypercholesterolemia, individuals who are homozygous for the mutation lack LDL cholesterol receptors in the liver, causing high levels of serum cholesterol.
 
  This is a defect in which type of gene pathway: a biosynthetic, signal transduction, or developmental pathway?
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Alonzoperez1118Alonzoperez1118
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